Halyard ANGIOGRAPHY DRAPE PACK — Class II medical device recall Z-0447-2025
Ongoing recall by AVID Medical, Inc., reported 2024-11-20, distributed nationwide. Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the com
| Recall number | Z-0447-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | AVID Medical, Inc., Toano, VA, United States |
| Recall initiated | 2024-09-20 |
| Classified | 2024-11-14 |
| Reported by FDA | 2024-11-20 |
| Distributed | Nationwide (US) |
| Quantity | 114 eaches |
| Reason classes | foreign material, device malfunction |
| UPC / GTIN / UDI-DI | 10809160334287 |
| Lot numbers | 1572642 |
| Model numbers | VMCC021-06 |
Product
Halyard ANGIOGRAPHY DRAPE PACK - Medical convenience kits Model Number: VMCC021-06
Reason for recall
Sponge forceps and towel clamps associated with small loose metal flakes potentially could detach from the components. Metal flakes on components may enter a patients surgical site undetected causing local reactions or possible foreign body reactions
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0447-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.